Access to the investigational treatment after the study ends depends on regulatory approvals. The study team will inform you of the next steps based on the trial’s outcomes.
This phase 2, double-blind, randomized Urinary Tract Infection Research Study aimed to evaluate the effectiveness of a new treatment in combination with antibiotics. The study focused on reducing the impact of drug-resistant E. coli infections in patients with active acute uncomplicated UTIs through innovative therapies.
In Part 1, the study assessed optimal dosing for the investigational drug among 30 participants, focusing on pharmacokinetics and safety. Part 2 involved randomly assigning participants to receive either the study drug + antibiotics or placebo + antibiotics, to evaluate the treatment’s efficacy and safety.
Not Recruiting
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Study Name | Protocol Number | Sponsor |
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Urinary Tract Infection | LBx-2001 | Locus Bioscience |
Access to the investigational treatment after the study ends depends on regulatory approvals. The study team will inform you of the next steps based on the trial’s outcomes.
No, pregnant or breastfeeding women are typically excluded from this study to ensure the safety of both the mother and child.
Yes, participants will be informed about the general findings once the study is completed, though individual results may not be shared. The research team can provide updates as they become available.